2-Bromodibenzothiophene 5,5-Dioxide

95%

Reagent Code: #147396
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CAS Number 53846-85-8

science Other reagents with same CAS 53846-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight ?295.15 g/mol
Formula C₁₂H₇BrO₂S
thermostat Physical Properties
Melting Point 267°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Heck reactions, to construct biaryl and heterobiaryl systems found in pharmaceuticals and functional materials. Its bromine functionality allows for selective metal-catalyzed substitutions, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive molecules. The sulfone group enhances electron-withdrawing properties and stability, which can improve performance in optoelectronic applications and as a building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,290.00
inventory 200mg
10-20 days ฿4,000.00
inventory 1g
10-20 days ฿18,270.00

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2-Bromodibenzothiophene 5,5-Dioxide
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Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Heck reactions, to construct biaryl and heterobiaryl systems found in pharmaceuticals and functional materials. Its bromine functionality allows for selective metal-catalyzed substitutions, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive molecules. The sulfone group enhances electron-withdrawing properties and stability, which can improve performance i

Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Heck reactions, to construct biaryl and heterobiaryl systems found in pharmaceuticals and functional materials. Its bromine functionality allows for selective metal-catalyzed substitutions, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive molecules. The sulfone group enhances electron-withdrawing properties and stability, which can improve performance in optoelectronic applications and as a building block in medicinal chemistry.

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